Askling J, Baecklund E, Granath F, Geborek P, Fored M, Backlin C, Bertilsson L, Cöster L, Jacobsson L T, Lindblad S, Lysholm J, Rantapää-Dahlqvist S, Saxne T, van Vollenhoven R, Klareskog L, Feltelius N
Department of Medicine, Clinical Epidemiology Unit, Karolinska Institutet at Karolinska University Hospital, Stockholm, Sweden.
Ann Rheum Dis. 2009 May;68(5):648-53. doi: 10.1136/ard.2007.085852. Epub 2008 May 8.
Tumour necrosis factor (TNF) antagonists have proved effective as treatment against rheumatoid arthritis (RA), but the unresolved issue of whether the use of anti-TNF therapy increases the already elevated risk of lymphoma in RA remains a concern.
Using the Swedish Biologics Register (ARTIS), the Swedish Cancer Register, pre-existing RA cohorts and cross-linkage with other national health and census registers, a national RA cohort (n = 67,743) was assembled and patients who started anti-TNF therapy between 1998 and July 2006 (n = 6604) were identified. A general population comparator (n = 471,024) was also assembled and the incidence of lymphomas from 1999 to 31 December 2006 was assessed and compared in these individuals.
Among the 6604 anti-TNF-treated RA patients, 26 malignant lymphomas were observed during 26,981 person-years of follow-up, which corresponded to a relative risk (RR) of 1.35 (95% CI 0.82 to 2.11) versus anti-TNF-naive RA patients (336 lymphomas during 365,026 person-years) and 2.72 (95% CI 1.82 to 4.08) versus the general population comparator (1568 lymphomas during 3,355,849 person-years). RA patients starting anti-TNF therapy in 1998-2001 accounted for the entire increase in lymphoma risk versus the two comparators. By contrast, RR did not vary significantly by time since start of first treatment or with the accumulated duration of treatment, nor with the type of anti-TNF agent.
Overall and as used in routine care against RA, TNF antagonists are not associated with any major further increase in the already elevated lymphoma occurrence in RA. Changes in the selection of patients for treatment may influence the observed risk.
肿瘤坏死因子(TNF)拮抗剂已被证明是治疗类风湿性关节炎(RA)的有效药物,但抗TNF治疗是否会增加RA患者本就已升高的淋巴瘤风险这一未解决问题仍令人担忧。
利用瑞典生物制剂登记册(ARTIS)、瑞典癌症登记册、既往RA队列以及与其他国家健康和人口普查登记册的交叉链接,组建了一个全国性RA队列(n = 67,743),并确定了1998年至2006年7月期间开始抗TNF治疗的患者(n = 6604)。还组建了一个普通人群对照组(n = 471,024),并评估和比较了这些个体在1999年至2006年12月31日期间淋巴瘤的发病率。
在6604例接受抗TNF治疗的RA患者中,在26,981人年的随访期间观察到26例恶性淋巴瘤,与未接受抗TNF治疗的RA患者(在365,026人年期间有336例淋巴瘤)相比,相对风险(RR)为1.35(95%CI 0.82至2.11),与普通人群对照组(在3,355,849人年期间有1568例淋巴瘤)相比为2.72(95%CI 1.82至4.08)。1998 - 2001年开始抗TNF治疗的RA患者与两个对照组相比,淋巴瘤风险全面增加。相比之下,RR并未因首次治疗开始后的时间、治疗的累积持续时间或抗TNF药物类型而有显著差异。
总体而言,在常规治疗RA中使用TNF拮抗剂与RA患者本就已升高的淋巴瘤发生率的任何进一步大幅增加无关。治疗患者选择的变化可能会影响观察到的风险。